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    AMBU® NEUTRALECT-MINI ELECTROSURGICAL NEUTRAL ELECTRODE

    FDA Adverse Event
    Injury ·AMBU A/S·Product code GEI·December 5, 2016

    AMBU NEUROLINE CONCENTRIC

    FDA Adverse Event
    Injury ·AMBU A/S·Product code IKT·September 11, 2015

    AMBU NEUROLINE 720

    FDA Adverse Event
    Other ·AMBU A/S·Product code GXY·February 24, 2012

    AMBU SPUR II

    FDA Adverse Event
    Death ·AMBU A/S·Product code BTM·May 9, 2014

    AMBU SPUR II ADULT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·AMBU A/S·Product code BTM·January 26, 2010

    SPUR II

    FDA Adverse Event
    Malfunction ·AMBU A/S·Product code BTM·January 4, 2010

    SPUR II

    FDA Adverse Event
    Malfunction ·AMBU A/S·Product code BTM·March 25, 2010

    AMBU NEUROLINE CONCENTRIC NEEDLE

    FDA Adverse Event
    Injury ·AMBU A/S·Product code IKT·April 30, 2010

    AMBU SPUR II

    FDA Adverse Event
    Injury ·AMBU A/S·Product code BTM·May 13, 2010

    AMBU AURASTRAIGHT DISPOSABLE LARYNGEAL MASK

    FDA Adverse Event
    Other ·AMBU A/S·Product code BTM·May 13, 2010

    SPUR® II INFANT RESUSCITATORSINGLE PATIENT USE RESUSCITATOR

    FDA Adverse Event
    Malfunction ·AMBU A/S·Product code BTM·October 4, 2017

    ASCOPE 4 BRONCHO REGULAR

    FDA Adverse Event
    Injury ·AMBU A/S·Product code EOQ·June 11, 2021

    ASCOPE 4 BRONCHO SLIM

    FDA Adverse Event
    Injury ·AMBU A/S·Product code EOQ·June 23, 2021

    ASCOPE 4 BRONCHO REGULAR

    FDA Adverse Event
    Injury ·AMBU A/S·Product code EOQ·May 19, 2021

    ASCOPE 4 BRONCHO LARGE

    FDA Adverse Event
    Injury ·AMBU A/S·Product code EOQ·June 4, 2021

    AMBU NEUROLINE CONCENTRIC NEEDLE

    FDA Adverse Event
    Injury ·AMBU A/S·Product code GXZ·June 8, 2021

    ASCOPE 4 BRONCHO LARGE

    FDA Adverse Event
    Injury ·AMBU A/S·Product code EOQ·June 30, 2021

    ASCOPE 4 BRONCHO SLIM

    FDA Adverse Event
    Injury ·AMBU A/S·Product code EOQ·June 22, 2021

    SPUR II PEDI. BAG RESVR

    FDA Adverse Event
    Death ·AMBU A/S·Product code BTM·May 18, 2021

    AURAFLEX

    FDA Adverse Event
    Injury ·AMBU A/S·Product code CAE·June 15, 2021